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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279068Generated: November 1, 2026

3-Bromo-6-chloroimidazo(1,2-b)pyridazine → 6-Chloro-3-(3-methoxypyridazin-4-yl)imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/2279068

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-6-chloroimidazo(1,2-b)pyridazineHCID 12872323—
Reactant3-Methoxy-4-(tributylstannyl)pyridazineHCID 67485729—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product6-Chloro-3-(3-methoxypyridazin-4-yl)imidazo[1,2-b]pyridazineHCID 8670232764.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-bromo-6-chloroimidazo[1,2-b]pyridazine (Preparation 1b, 182 mg, 0.78 mmol), 3-methoxy-4-(tributylstannyl)pyridazine (Preparation 8b, 313 mg, 0.78 mmol), copper(I) iodide (15 mg, 0.08 mmol) and dry N,N′-dimethylformamide (4 mL) in a Schlenk vial was subjected to three cycles of evacuation backfilling with argon. Tetrakis(triphenylphosphine)palladium(0) (91 mg, 0.08 mmol) was then added and the resulting mixture was subjected to three further cycles of evacuation backfilling with argon before being stirred at 100° C. for 20 hours. The reaction mixture was cooled down, the solvent was removed under reduced pressure and the residue was purified by flash chromatography (1:1 hexanes/ethyl acetate to 100% ethyl acetate) to give the title compound (131 mg, 64%) as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133200B2
Source datasetuspto-grants-2015_09
ORD IDord-6d5d64b71fbf48d6a37a2caf250cbbf9
Source noteuspto-grants-2015_09